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International Journal of Hematology
|
September 4, 2025
Sequential occurrence of BCR::ABL1-negative MPN and CML and vice versa: results from a real world cohort
Katrin Schweneker, Miriam Lenk, Wolfgang Kern, et al.
Cancer Genetics
|
November 8, 2019
Cytogenetic and molecular genetic characterization of KMT2A-PTD positive acute myeloid leukemia in comparison to KMT2A-Rearranged acute myeloid leukemia
Calogero Vetro, Torsten Haferlach, Manja Meggendorfer, et al.
British Journal of Haematology
|
July 23, 2016
Application of an NGS-based 28-gene panel in myeloproliferative neoplasms reveals distinct mutation patterns in essential thrombocythaemia, primary myelofibrosis and polycythaemia vera
Sabit Delic, Dominic Rose, Wolfgang Kern, et al.
Cancer Genetics
|
May 20, 2025
Potential factors underlying the progression of RUNX1-mutated MDS to AML
Anna Stengel, Katharina Hörst, Constanze Kühn, et al.
BMC Cancer
|
August 3, 2021
Clinical application of whole transcriptome sequencing for the classification of patients with acute lymphoblastic leukemia
Wencke Walter, Rabia Shahswar, Anna Stengel, et al.
Blood Reviews
|
October 14, 2022
Artificial intelligence in hematological diagnostics: Game changer or gadget?
Wencke Walter, Christian Pohlkamp, Manja Meggendorfer, et al.
Haematologica
|
April 10, 2025
Acute pro-B-cell lymphoblastic leukemia evolving from myelodysplastic neoplasm post cytotoxic therapy: a case report
Jana Wobst, Marietta Truger, Constance Baer, et al.
Hemasphere
|
November 15, 2019
Molecular characterization of AML with <i>RUNX1-RUNX1T1</i> at diagnosis and relapse reveals net loss of co-mutations
Alexander Höllein, Niroshan Nadarajah, Manja Meggendorfer, et al.
Blood Advances
|
September 27, 2021
Mutational patterns and their correlation to CHIP-related mutations and age in hematological malignancies
Anna Stengel, Constance Baer, Wencke Walter, et al.
Cytometry. Part B, Clinical Cytometry
|
January 28, 2022
Identification of a specific immunophenotype associated with a consistent pattern of genetic mutations including SRFS2 and gene expression profile in MDS
Elisabeth Weiß, Wencke Walter, Manja Meggendorfer, et al.
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of 13
Search research articles
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Showing results (11-20 of 125) with videos related to
Sort By:
Page
of 13
International Journal of Hematology
|
September 4, 2025
Sequential occurrence of BCR::ABL1-negative MPN and CML and vice versa: results from a real world cohort
Katrin Schweneker, Miriam Lenk, Wolfgang Kern, et al.
Cancer Genetics
|
November 8, 2019
Cytogenetic and molecular genetic characterization of KMT2A-PTD positive acute myeloid leukemia in comparison to KMT2A-Rearranged acute myeloid leukemia
Calogero Vetro, Torsten Haferlach, Manja Meggendorfer, et al.
British Journal of Haematology
|
July 23, 2016
Application of an NGS-based 28-gene panel in myeloproliferative neoplasms reveals distinct mutation patterns in essential thrombocythaemia, primary myelofibrosis and polycythaemia vera
Sabit Delic, Dominic Rose, Wolfgang Kern, et al.
Cancer Genetics
|
May 20, 2025
Potential factors underlying the progression of RUNX1-mutated MDS to AML
Anna Stengel, Katharina Hörst, Constanze Kühn, et al.
BMC Cancer
|
August 3, 2021
Clinical application of whole transcriptome sequencing for the classification of patients with acute lymphoblastic leukemia
Wencke Walter, Rabia Shahswar, Anna Stengel, et al.
Blood Reviews
|
October 14, 2022
Artificial intelligence in hematological diagnostics: Game changer or gadget?
Wencke Walter, Christian Pohlkamp, Manja Meggendorfer, et al.
Haematologica
|
April 10, 2025
Acute pro-B-cell lymphoblastic leukemia evolving from myelodysplastic neoplasm post cytotoxic therapy: a case report
Jana Wobst, Marietta Truger, Constance Baer, et al.
Hemasphere
|
November 15, 2019
Molecular characterization of AML with <i>RUNX1-RUNX1T1</i> at diagnosis and relapse reveals net loss of co-mutations
Alexander Höllein, Niroshan Nadarajah, Manja Meggendorfer, et al.
Blood Advances
|
September 27, 2021
Mutational patterns and their correlation to CHIP-related mutations and age in hematological malignancies
Anna Stengel, Constance Baer, Wencke Walter, et al.
Cytometry. Part B, Clinical Cytometry
|
January 28, 2022
Identification of a specific immunophenotype associated with a consistent pattern of genetic mutations including SRFS2 and gene expression profile in MDS
Elisabeth Weiß, Wencke Walter, Manja Meggendorfer, et al.
Page
of 13